Canonical Allele Identifier: PA916027722
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 208163
ClinVar RCV Id: RCV000206266 RCV000312203 RCV000821003
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316079.1:p.His68Arg
CA339766
NM_001329150.2:c.203A>G